Literature DB >> 8401494

Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping.

D L Neil1, A J Jeffreys.   

Abstract

Minisatellite variant repeat unit mapping by PCR (MVR-PCR) assays the interspersion pattern of variant repeat units along minisatellite alleles. Mapping such internal variation in the highly polymorphic minisatellite MS31A (locus D7S21), reveals extreme levels of allelic variability, far in excess of that detectable by allele length analysis. Flanking base substitutional polymorphisms have enabled the 5' structure of large numbers of MS31A alleles to be derived from genomic DNA by allele-specific MVR-PCR. More than 100 alleles have now been mapped and all are different. Several alleles show related internal structures and some of these provide evidence of polarity in allelic variation reminiscent of that seen at two other hypervariable minisatellites, D1S8 (MS32) and D16S309 (MS205). We also describe the diploid digital coding of MS31A, including the simultaneous coding of MS31A and a second locus, MS32, by duplex MVR-PCR, which greatly enhances the potential forensic applications of this technique.

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Year:  1993        PMID: 8401494     DOI: 10.1093/hmg/2.8.1129

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  12 in total

1.  Minisatellite MS32 alleles show population specificity among Thai, Chinese, and Japanese.

Authors:  Qing-Hua Yuan; Azusa Tanaka; Richard H Kaszynski; Morio Iino; Tomoko Okuno; Tatsuaki Tsuruyama; Toshimichi Yamamoto; Alec J Jeffreys; Keiji Tamaki
Journal:  J Mol Evol       Date:  2009-01-22       Impact factor: 2.395

2.  Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array.

Authors:  R Andreassen; T Egeland; B Olaisen
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

3.  Short alleles revealed by PCR demonstrate no heterozygote deficiency at minisatellite loci D1S7, D7S21, and D12S11.

Authors:  S Alonso; A Castro; I Fernández-Fernández; M M de Pancorbo
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

4.  VNTR alleles associated with the alpha-globin locus are haplotype and population related.

Authors:  J J Martinson; A J Boyce; J B Clegg
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025

5.  A general method for the detection of large CAG repeat expansions by fluorescent PCR.

Authors:  J P Warner; L H Barron; D Goudie; K Kelly; D Dow; D R Fitzpatrick; D J Brock
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

6.  Ha-ras rare alleles in breast cancer susceptibility.

Authors:  K Conway; S Edmiston; D B Fried; B S Hulka; P A Garrett; E T Liu
Journal:  Breast Cancer Res Treat       Date:  1995-07       Impact factor: 4.872

7.  Tandemly repeated transgenes of the human minisatellite MS32 (D1S8), with novel mouse gamma satellite integration.

Authors:  M J Allen; A J Jeffreys; M A Surani; S Barton; M L Norris; A Collick
Journal:  Nucleic Acids Res       Date:  1994-08-11       Impact factor: 16.971

8.  Repeat instability at human minisatellites arising from meiotic recombination.

Authors:  A J Jeffreys; D L Neil; R Neumann
Journal:  EMBO J       Date:  1998-07-15       Impact factor: 11.598

9.  Mechanisms underlying telomere repeat turnover, revealed by hypervariable variant repeat distribution patterns in the human Xp/Yp telomere.

Authors:  D M Baird; A J Jeffreys; N J Royle
Journal:  EMBO J       Date:  1995-11-01       Impact factor: 11.598

10.  Variable germline and embryonic instability of the human minisatellite MS32 (D1S8) in transgenic mice.

Authors:  A Collick; M L Norris; M J Allen; P Bois; S C Barton; M A Surani; A J Jeffreys
Journal:  EMBO J       Date:  1994-12-01       Impact factor: 11.598

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